Replication Origins: Why Do We Need So Many?
Overview
Authors
Affiliations
During the G1 phase of the cell cycle, replication origins are prepared to fire, a process that is referred to as origin licensing. It was often pondered what a cell's fate would be if not all of its replication origins were licensed and subsequently activated during S phase. One obvious prediction was that S phase would simply be prolonged. As it turns out, however, the consequences are much more complex. A short G1 phase enforced by premature entry into S phase, or other events that negatively affect origin licensing, will ultimately compromise the cell's ability to complete DNA replication before entering mitosis. As a result, the cell becomes genomically unstable when it attempts to repair unreplicated DNA during anaphase. Thus, the density of active replication origins in the chromosomes of eukaryotic cells determines S phase dynamics and chromosome stability during mitosis.
Mcm10: A Dynamic Scaffold at Eukaryotic Replication Forks.
Baxley R, Bielinsky A Genes (Basel). 2017; 8(2).
PMID: 28218679 PMC: 5333062. DOI: 10.3390/genes8020073.
Order from clutter: selective interactions at mammalian replication origins.
Aladjem M, Redon C Nat Rev Genet. 2016; 18(2):101-116.
PMID: 27867195 PMC: 6596300. DOI: 10.1038/nrg.2016.141.
Zhang Y, Huang L, Fu H, Smith O, Lin C, Utani K Nat Commun. 2016; 7:11748.
PMID: 27272143 PMC: 4899857. DOI: 10.1038/ncomms11748.
Penetrating enemy territory: Soluble PCNA-peptides stress out MYCN-overexpressing neuroblastomas.
Bielinsky A EBioMedicine. 2016; 2(12):1844-5.
PMID: 26844252 PMC: 4703722. DOI: 10.1016/j.ebiom.2015.12.012.
Bua S, Sotiropoulou P, Sgarlata C, Borlado L, Eguren M, Dominguez O Cell Cycle. 2015; 14(24):3897-907.
PMID: 26697840 PMC: 4825757. DOI: 10.1080/15384101.2015.1120919.